Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/4904
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Type: Journal article
Title: Aryl nitrile oxide cycloaddition reactions in the presence of baker's yeast and β-cyclodextrin
Other Titles: Aryl nitrile oxide cycloaddition reactions in the presence of baker's yeast and beta-cyclodextrin
Author: Easton, Christopher J.
Hughes, Christine Merricc M.
Tiekink, Edward Richard Tom
Savage, G. Paul
Simpson, George W.
Citation: Tetrahedron Letters. 36:629-632
Publisher: Pergamon Press
Issue Date: 1995
ISSN: 0040-4039
School/Discipline: School of Chemistry and Physics
School of Chemistry and Physics : Chemistry
Statement of
Responsibility: 
Christopher J. Easton, C. Merrîcc, M. Hughes, Edward R.T. Tiekink, G. Paul Savage, Gregory W. Simpson
Abstract: Contrary to recent reports, baker's yeast is not required for reactions of nitrile oxides with either ethyl cinnamate or 4-vinylpyridine to give isoxazolines. β-Cyclodextrin may alter the ratio of isomers isolated from the reactions of the cinnamate but only at concentrations of reactants much lower than those reported, and this effect is most likely due to selective product complexation rather than selective product formation.
Rights: Copyright © 1995 Published by Elsevier Ltd.
DOI: 10.1016/0040-4039(94)02321-2
Appears in Collections:Chemistry publications

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